3208-26-2

Basic information

• Product Name: 9-PHENYL-1-NONANOL
• Synonyms: 9-PHENYLNONANOL;9-PHENYL-1-NONANOL;9-Phenyl-1-nonanol,97%;9-Phenylnonan-1-ol
• CAS NO: 3208-26-2
• Molecular Formula: C₁₅H₂₄O
• Molecular Weight: 220.35
• Mol File: 3208-26-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 125-127°C 0,1mm
• Flash Point: 125-127°C/0.1mm
• Appearance: /
• Density: 0.936 g/cm³
• Vapor Pressure: 7.68E-05mmHg at 25°C
• Refractive Index: 1.5030
• PKA: 15.20±0.10(Predicted)
• BRN: 2521084
• CAS DataBase Reference: 9-PHENYL-1-NONANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 9-PHENYL-1-NONANOL(3208-26-2)
• EPA Substance Registry System: 9-PHENYL-1-NONANOL(3208-26-2)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 3208-26-2(Hazardous Substances Data)

Usage

General Description

9-PHENYL-1-NONANOL is a chemical compound that belongs to the class of alcohols. It is a colorless to pale yellow liquid with a floral odor and is commonly used as a fragrance ingredient in various personal care and household products. 9-PHENYL-1-NONANOL has the molecular formula C15H24O and is often used in the production of perfumes, soaps, and cosmetics due to its pleasant smell and ability to enhance the overall fragrance profile of a product. Additionally, it can act as a solvent or viscosity decreasing agent in a variety of formulations, making it a versatile and frequently utilized compound in the fragrance and personal care industries.

InChI:InChI=1/C15H24O/c16-14-10-5-3-1-2-4-7-11-15-12-8-6-9-13-15/h6,8-9,12-13,16H,1-5,7,10-11,14H2

Upstream product

• 4280-89-1 1-(α-furyl)-5-phenylpenta-1,4-dien-3-one 
• 16269-06-0 9-phenylnonanoic acid 
• 24197-55-5 9-phenylnonanoic acid methyl ester 
• 117806-56-1 2-(9-Phenyl-nonyloxy)-tetrahydro-pyran 
• 55695-90-4 2-(9-bromononyloxy)tetrahydropyran 
• 100-58-3 phenylmagnesium bromide 
• 4224-63-9 6-iodohexanoic acid 
• 14273-91-7 methyl 6-iodohexanoate 
• 637-59-2 1-Bromo-3-phenylpropane 
• 116384-96-4 5-benzylthiophen-2-butanoic acid 
• 13132-15-5 2-benzylthiophene 
• 116384-95-3 methyl 5-benzyl-γ-oxothiophen-2-butanoate 
• 120756-17-4 9-(phenyl)-nonanoic acid ethyl ester 
• 3208-25-1 7-phenylheptan-1-ol 

Downstream Products

• 103602-67-1 9-phenyl-1-bromononane 
• 221656-52-6 N,N-dimethyl-9-phenylnonylamine 
• 221656-94-6 N-methyl-9-phenyl-n-nonylamine 
• 221657-01-8 N-benzyl-N-methyl-9-phenyl-n-nonylamine 
• 221656-95-7 N-methyl,N-(9-phenyl-n-nonyl)-9-phenyl-n-nonylamine 
• 221656-97-9 N-methyl-N-(3,7,11-trimethyl-2(E),6(E),10-dodecatrienyl)-9-phenyl-n-nonamine 
• 221657-05-2 N,N'-bis(methyl-9-phenylnonyl)ethylenediamine 
• 206647-08-7 (4R,5R)-4-Methyl-5-(3-oxo-12-phenyl-dodecyl)-oxazolidin-2-one 
• 206647-04-3 (4R,5R)-3-Benzyl-5-(3-hydroxy-12-phenyl-dodecyl)-4-methyl-oxazolidin-2-one 
• 24065-64-3 1,18-diphenyloctadecane 
• 177706-80-8 4-oxo-13-phenyltridecanoic acid 

Relevant articles and documents

DITERPENOID COMPOUNDS THAT ACT ON PROTEIN KINASE C (PKC)

This present disclosure relates to protein kinase C (PKC) modulating compounds, methods of treating a subject with cancer using the compounds, and combination treatments with a second therapeutic agent.

Synthesis and biological evaluation of some undecanone derivatives

The total synthesis of Ardisinone E [15, 1-(2,4,6-trihydroxy phenyl)-11-(2-hydroxyphenyl)-undecan-1-one], a natural diarylundecanone, isolated from Ardisia arborescens, was accomplished along with 16 new diarylundecanone analogs (18a–p), by modified Wittig reaction. The structures of the compounds were confirmed by 1H, 13C and mass spectral data. Compound 15 showed potent cytotoxic activity with an ED50 of 4.19 μg/mL in brine shrimp lethality assay model. Compounds 18c, 18e, 18j, 18k, 18l, and 18m exhibited strong anti-oxidant activity with IC50 values of 18.75, 12.28, 18.35, 11.04, 12.05, and 11.32 μg/mL, respectively, in NBT free radical assay. Compounds 18e, 18k, and 18m also showed significant 5-lipoxyganase enzyme inhibitory potential with IC50 values of 12.8, 15.23, and 15.23 μg/mL, respectively.

Enantioselective total synthesis of Irniine and Bgugaine, bioactive 2-alkylpyrrolidine alkaloids

An asymmetric total synthesis of the 2-(R)-alkylpyrrolidines, (-)-irniine (1a) and (-)-bgugaine (1b), toxic and antibiotic components of the tubers of Arisarum vulgare, and (+)-(S)-irniine (1c), was carried out by condensation of the corresponding 4-oxoalkanoic acid (9) with chiral phenylglycinol. Acids (9) were prepared from a hetero-organocuprate (I) complex, generated by reaction of methylcopper (I) with alkylmagnesium bromides and methyl chlorocarbonylpropionate. Alkaloids (1a, 1b and 1c) displayed anti Gram(+) bacterial (MIC 12.5 - 50 μg/ml) and antifungal (MIC 6.25 - 50 μg/ml) activities.